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Biological consequences of irradiation by low doses of technetium 99m: ultrastructural studies, p53 protein expression and cytogenetic effects.

机译:低剂量99 99m辐射的生物学后果:超微结构研究,p53蛋白表达和细胞遗传学效应。

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摘要

Few studies concerning the potential genetic effects of diagnostic radionuclides used in nuclear medicine have been reported. The aim of this study was to evaluate the biological and cytogenetic consequences of two technetium 99m-labelled radiopharmaceuticals. Ultrastructural modifications of pulmonary cells were first investigated after injection of 99mTc labelled microspheres in the rat. On the same irradiated cells, nuclear expression of p53 protein was assessed using immunohistochemistry. Despite very high previously calculated doses delivered to pulmonary cells, no morpholological cell damage and no significant increase of nuclear expression of the p53 were noted. There was no correlation between the calculated dose and the ultrastructural biological damage. Secondly, a specific in vitro curve, activityumber of unstable chromosomal aberrations, corresponding to physical characteristics of 99mTc, was established to verify the potentiality of 99mTc to induce such aberrations. In vivo, cytogenetic effects were assessed on blood samples of 5 patients with various arthrosic and periarthrosic diseases obtained after bone scintigraphy. Aberration frequencies of both in vitro and in vivo irradiated lymphocytes were determined using the classical Fluorescence Plus Giemsa technique. No cytogenetic effects appeared with the routinely 99mTc injected activities as predicted by the in vitro curve.
机译:关于核医学中使用的诊断性放射性核素的潜在遗传效应的研究鲜有报道。这项研究的目的是评估两种tech 99m标记的放射性药物的生物学和细胞遗传学后果。在大鼠中注射99mTc标记的微球后,首先研究了肺细胞的超微结构修饰。在相同的照射细胞上,使用免疫组织化学评估了p53蛋白的核表达。尽管事先计算出非常高的剂量递送给肺细胞,但未观察到形态学上的细胞损伤和p53核表达的显着增加。计算剂量与超微结构生物学损伤之间没有相关性。其次,建立了一条特定的体外曲线,即与99mTc物理特征相对应的不稳定染色体畸变的活性/数目,以验证99mTc诱导此类畸变的潜力。在体内,对骨闪烁显像后获得的5例患有各种关节炎和关节炎的患者的血液样本进行了细胞遗传学评估。使用经典的Fluorescence Plus Giemsa技术确定体外和体内照射的淋巴细胞的像差频率。如体外曲线所预测的,常规的99mTc注射活性没有细胞遗传学作用。

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